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Results 1 - 10 of 93 for Congenital blindness
  1. Autosomal recessive congenital stationary night blindness 
    Autosomal recessive congenital stationary night blindness is a disorder of the retina, which is the specialized tissue at the back of the eye that detects light ...
    https://medlineplus.gov/...ive-congenital-stationary-night-blindness - Genetics
  2. Autosomal dominant congenital stationary night blindness 
    ... Kraft TW, Gross AK. 1 rhodopsin mutations in congenital night blindness. Adv Exp Med Biol. 2010;664:263-72. ...
    https://medlineplus.gov/...ant-congenital-stationary-night-blindness - Genetics
  3. X-linked congenital stationary night blindness 
    X-linked congenital stationary night blindness is a disorder of the retina, which is a specialized tissue at the back of the eye that ... typically not affected in people with X-linked congenital stationary night blindness.The vision problems associated with X-linked congenital ...
    https://medlineplus.gov/...ked-congenital-stationary-night-blindness - Genetics
  4. Leber congenital amaurosis 
    ... Amaurosis, Leber congenital Congenital amaurosis of retinal origin Congenital retinal blindness CRB Dysgenesis neuroepithelialis retinae Hereditary epithelial dysplasia of ...
    https://medlineplus.gov/.../condition/leber-congenital-amaurosis - Genetics
  5. Visual Impairment (Nemours Foundation)  
    ... loss, visual problems, eyes, eyesight, sight, sigt, seeing, congenital blindness, retina, cornea, iris, lens, braille, eye injuries, seeing-eye dog, seeing-eye dogs, guide dog, ...
    https://kidshealth.org/en/teens/visual-impairment.html - External Health Links
  6. RHO gene 
    ... Kraft TW, Gross AK. 1 rhodopsin mutations in congenital night blindness. Adv Exp Med Biol. 2010;664:263-72. ...
    https://medlineplus.gov/genetics/gene/rho - Genetics
  7. NYX gene 
    ... have been identified in people with X-linked congenital stationary night blindness. NYX gene variants are responsible for the complete ... which impairs vision in people with X-linked congenital stationary night blindness. The rod pathway is severely disrupted, while the ...
    https://medlineplus.gov/genetics/gene/nyx - Genetics
  8. CACNA1F gene 
    ... have been identified in people with X-linked congenital stationary night blindness. CACNA1F gene variants are responsible for the incomplete ... which impairs vision in people with X-linked congenital stationary night blindness. More About This Health Condition MedlinePlus Genetics provides ...
    https://medlineplus.gov/genetics/gene/cacna1f - Genetics
  9. TRPM1 gene 
    ... gene have been found to cause autosomal recessive congenital stationary night blindness, which is characterized by the inability to see ... is mutated in patients with autosomal-recessive complete congenital stationary night blindness. Am J Hum Genet. 2009 Nov;85(5): ...
    https://medlineplus.gov/genetics/gene/trpm1 - Genetics
  10. GRM6 gene 
    ... gene have been found to cause autosomal recessive congenital stationary night blindness, which is characterized by the inability to see ... coupling in an mGluR6 point mutant associated with congenital stationary night blindness. Mol Pharmacol. 2009 Nov;76(5):992-7. ...
    https://medlineplus.gov/genetics/gene/grm6 - Genetics
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